Thin film capacitor and fabrication method thereof

ABSTRACT

A thin film capacitor comprising a top electrode, a bottom electrode, and a dielectric film held between the top and bottom electrodes. The dielectric film is composed of at least cations Ba, Sr, and Ti and anion O. The concentration of Sr, Ti, and O ions are uniform along the growth direction of the dielectric film while the concentration of the Ba cation is non-uniform along the growth direction such that a reduced Ba-I region in which the average concentration of perovskite type Ba cations (Ba-I) is less than the average concentration of non-perovskite type Ba cations (Ba-II) exists at or near the boundary between at least one of the top and bottom electrodes, with ratio R=(atm % Ba-I)/[(atm % Ba-I)+(atm % Ba-II)] within a range of 0.1&lt;R&lt;0.2.

This application is a divisional of application Ser. No. 11/582,480,filed Oct. 18, 2006.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates in general to a thin film capacitor, andmore particularly, to a thin film capacitor using a perovskite typedielectric film with a specific distribution profile along the growthdirection, which capacitor is capable of reducing electric currentleakage and enhancing service life of devices.

2. Description of the Related Art

Thin film ABO₃ perovskite type dielectric materials, such as bariumstrontium titanate (BST: (Ba,Sr)TiO₃), are currently being investigatedfor applications in microwave and RF devices and as charge storagedevices for decoupling capacitor and DRAM applications. For theseapplications a high capacitance density, low leakage current, reduceddielectric loss, and long service life are required.

One of the major problems impeding the use of polycrystalline highdielectric constant oxide thin films, such as (Ba,Sr)TiO₃, in deviceapplications is achieving capacitance densities sufficient for deviceapplications while maintaining low leakage with good service life.

Japanese Patent Registration No. 2929435 (corresponding to U.S. Pat. No.5,783,253) discloses a technique for forming a dielectric film withimproved physical and electrical characteristics, achieving a higherdielectric constant and smooth surfaces. With this method, a first BSTfilm of a Barium composition x (Ba_(x)Sr_(1-x)) is formed, and then asecond BST film of a different Ba composition x′ (x′=0.5)(Ba_(0.5)Sr_(0.5)) is formed over the first BST film. The first BST filmserves to improve the surface roughness, and the second BST film servesto achieve a higher dielectric constant.

SUMMARY OF THE INVENTION

The present invention was conceived in view of the above-describedproblems, especially of miniaturized device applications, and theembodiments provide a novel structure of a thin film capacitor withreduced leakage current density and enhanced capacitor service life.

To be more precise, the present invention utilizes a novel gradedchemical composition structure where the Ba cation is non-uniform in thesurface region of a dielectric (BST) film such that the averageconcentration ratio of perovskite type Ba cations (Ba-I) to the averageconcentration ratio of non-perovskite type Ba cations (Ba-II) is lessthan unity (e.g., less than 1) within a certain depth from the topsurface.

In one aspect of the invention, a thin film capacitor comprises a topelectrode, a bottom electrode, and a dielectric film located between thetop and the bottom electrodes and comprised of at least the cations Ba,Sr, Ti and anion O. The concentration of Sr, Ti, and O ions are uniformalong the growth direction of the dielectric film. The dielectric filmhas a reduced Ba-I region at or near the boundary between the dielectricfilm and at least one of the top and bottom electrodes, in which theaverage concentration of perovskite type Ba cations (Ba-I) is less thanthe average concentration of non-perovskite type Ba cations (Ba-II), andin which the average concentration ratio R is within the range of0.1<R<0.2, where R is (atm % Ba-I)/[(atm % Ba-I)+(atm % Ba-II)].

In another aspect of the invention, a method of fabricating a thin filmcapacitor is provided. The method comprises the steps of:

(a) forming over a bottom electrode a dielectric film comprised of atleast Ba, Sr, Ti, and O ions at certain compositions; and

(b) when forming a top electrode over the dielectric film, controlling acondition of film deposition of the top electrode so as to produce areduced Ba-I region in a surface region of the dielectric film in whichthe average concentration of perovskite-type Ba cations (Ba-I) is lessthan the average concentration ratio of non-perovskite type Ba cations(Ba-II).

In a preferred example, the film deposition of the top electrode iscontrolled such that the average concentration ratio R is within rangeof 0.1<R<0.2, where R is (atm % Ba-I)/[(atm % Ba-I)+(atm % Ba-II)].

In another preferred example, after the fabrication of the topelectrode, annealing is performed at 100-900° C. in an oxygen atmosphereto adjust the R value. This arrangement can efficiently reduce theleakage current density.

With the above-described structure and method, the leakage currentdensity of a thin film capacitor can be reduced and the device servicelife is enhanced.

BRIEF DESCRIPTION OF THE DRAWINGS

Other objects, features, and advantages of the present invention willbecome more apparent from the following detailed description when readin conjunction with the accompanying drawings, in which:

FIG. 1 is a schematic cross-sectional diagram of a thin film capacitoraccording to an embodiment of the invention;

FIG. 2 is a schematic diagram for explaining angle resolved X-rayphotoelectron spectroscopy (ARXPS) for measuring the concentrationdistribution of ions along the growth direction of the reduced Ba-Iregions of a BST dielectric film according to an embodiment of theinvention;

FIG. 3A through FIG. 3D are graphs showing the ARXPS measurementresults;

FIG. 4A and FIG. 4B are angle resolved XPS data showing that the R valuecan be controlled by top Pt film deposition over the BST dielectricfilm;

FIG. 5A through FIG. 5C are schematic diagram illustrating chemicalshift, relative ratio of Ba-I concentration to Ba-II concentration, andthe physical structure near the interface of a Pt/BST sample,respectively;

FIG. 6A and FIG. 6B are schematic cross-sectional diagrams illustratingR-value control by annealing;

FIG. 7A through FIG. 7E are schematic cross-sectional diagramsillustrating a fabrication process of a semiconductor device with a thinfilm capacitor; and

FIG. 8 is a graph showing the leak current density reducing effectachieved by controlling of the Ba-I relative concentration.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

The preferred embodiments of the invention are now described inconjunction with the attached drawings.

FIG. 1 is a schematic cross-sectional diagram of a thin film capacitor10 illustrated as an example of integrated thin film devices. The thinfilm capacitor 10 has a bottom electrode 12, a top electrode 14, and adielectric film 13 inserted between the bottom and top electrodes 12 and14. The dielectric film 13 is comprised of at least Ba, Sr and Tications and O anions. Ba cations have a specific concentration profilein the surface area along the growth direction, while Sr, Ti and O ionshave constant distribution profiles in the dielectric film 13.

To be more precise, the dielectric film 13 includes a reduced Ba-Iregion 13 a located in the surface area, and a bulk region 13 b withconstant compositions. In the reduced Ba-I region 13 a, the averageconcentration ratio [atom %] of perovskite type Barium ions (referred toas “Ba-I”) is less than the average concentration ratio ofnon-perovskite type Barium ions (referred to as “Ba-II”). The relativeconcentration ratio R of Ba-I is expressed asR=(Ba-I atom %)/[(Ba-I atom %)+(Ba-II atom %)],and R is within the range of 0.1<R<0.2. In the example shown in FIG. 1,R is 0.14 (R=0.14).

The reduced Ba-I region 13 a extends to 5 nm depth, and more preferably,to 2.5 nm depth, from the boundary face (interface) between the topelectrode 14 and the dielectric film 13. The compositions of Sr, Ti, andO are constant even in the reduced Ba-I region 13 a, as in the bulkregion 13 b. In the bulk region 13 b, the composition is(Ba_(0.7)Sr_(0.3))TiO₃.

FIG. 2 is a schematic diagram for explaining angle resolved X-rayphotoelectron spectroscopy (ARXPS) used to measure the ion concentrationof a sample with a reduced Ba-I region in the surface area.

Upon irradiation of X-rays onto the sample in a vacuum, photoelectrons(secondary electrons) existing in the region of up to 5 nm to 6 nm depthof the sample are emitted from the sample surface. The takeoff angle(i.e., the detection angle) is varied to measure the energies of thephotoelectrons and the number of photoelectrons (i.e., the intensity)ejected from the inner shells of the atoms contained in the sample. Fromthe analysis of the ARXPS measurement, what kinds of atoms exist in whatphases at which locations (depths from the sample surface) can bedetermined.

In the example shown in FIG. 2, photoelectrons are detected at takeoffangles of 30° and 90° to measure the ion concentrations of Ba, Sr, Tiand O at 2.5-nanometer depth and 5.0-nanometer depth, respectively, fromthe surface. From the measurement the concentration and chemical statesof Ba, Sr, Ti cations can be determined.

FIG. 3A through FIG. 3D are graphs of the ARXPS measurement results. Inthe graphs, the solid lines represent the XPS spectrums for the30-degree takeoff angle (at a shallow location), and the dashed linesrepresent the XPS spectrums for the 90-degree takeoff angle (at a deeplocation). FIG. 3A shows the photoelectron spectrums from the 3delectron trajectory of Ba, FIG. 3B shows those from the 3d electrontrajectory of Sr, FIG. 3C shows those from the 1s electron trajectory ofO, and FIG. 3 d shows those from the 2p electron trajectory of Ti. Achemical shift is observed in the Ba 3d lines, while the other elementsSr, Ti and O show no chemical shift with angle dependence and areuniform along the growth direction.

In the Ba 3d spectrums in FIG. 3A, the right-side-hand peak is of spin5/2, and the left-hand-side peak is of spin 3/2. Each peak is acombination of Ba ions of different phases, that is, perovskite-phaseBa-I and non-perovskite-phase Ba-II, as illustrated in FIG. 4A and FIG.4B.

FIG. 4A and FIG. 4B show that the concentration ratio of Ba ions in theperovskite phase (Ba-I) can be controlled with respect to Ba ions in thenon-perovskite phase (Ba-II) through film deposition of the top Ptelectrode 14 over the BST film 13.

From the ARXPS data of a BST sample (without a Pt film over it) for the30-degree takeoff angle shown in FIG. 4A, the binding energy of Ba-I,which spectrum is represented by the dotted broken line, is lower thanthe binding energy of Ba-II, which spectrum is represented by the solidline. For the spin 5/2 peak, the binding energy of Ba-I is 778 eV, andthat of Ba-II is 779.4 eV. The Ba-I concentration is double the Ba-IIconcentration.

In contrast, from the ARXPS data of a Pt/BST sample shown in FIG. 4B, inwhich a Pt film is formed over the BST film formed under the control ofdeposition conditions, the concentration ratio of Ba-I relative to Ba-IIhas been altered such that the Ba-I concentration becomes much less thanthe Ba-II concentration. To control the deposition conditions during theformation of the Pt film over the BST film, the power and/or thepressure may be adjusted so as to introduce defects in the surface areaof the BST film (which defects increase non-perovskite-phase Ba-IIrelative to perovskite-phase Ba-I). Thus, it is understood from FIG. 4Aand FIG. 4B that the Ba-I concentration can be reduced with respect tothe Ba-II concentration in the surface area of the BST film through theformation of the Pt film over the BST film under certain conditions.

The relative ratio of Ba-I to Ba-II can also be controlled to a desiredvalue by performing acid cleaning on the BST surface prior to formingthe Pt film to remove Ba-II while leaving the Ba-I component, and thenforming a Pt film over the cleaned surface of the BST film. Thisarrangement can reduce the Ba-I concentration in the surface area of theBST film, relative to the Ba-II concentration therein.

FIG. 5A through FIG. 5C are ARXPS data and the physical structure of aPt/BST sample. The ARXPS spectra of FIG. 5A show the Ba-I concentrationreduced relative to the Ba-II concentration in the surface area(measured at 30-degree take off) of the BST film, which profiles areachieved by forming a Pt film over the BST film under the control ofdeposition conditions. The table of FIG. 5B shows the Ba-I counts andthe Ba-II counts of 3d electron trajectory and the relativeconcentration ratio R at the ejection angle of 30 degrees. In thereduced Ba-I region 13 a of the BST film 13 located near the interfacewith the Pt film 14 shown in FIG. 5C, the concentration ofperovskite-phase Ba ions (Ba-I) is reduced such that the relative ratioR become 0.14. In contrast, the remaining atoms Sr, Ti, and O maintainsubstantially constant compositions throughout the BST film 13. Thisfilm structure is effective to reduce electric current leakage at ornear the boundary between the dielectric film and the electrode.

The relative intensities of perovskite-phase Ba-I andnon-perovskite-phase Ba-II can be further controlled by annealingtreatment, as illustrated in FIG. 6A and FIG. 6B. For example, thereduced Ba-I region 53 a with R value of 0.12 is produced in the surfacearea of the BST dielectric film 13 through the deposition of a Pt filmunder the controlled conditions, as illustrated in FIG. 6A. Then,annealing treatment is performed in the temperature range of 100° C. to900° C. in an oxygen atmosphere for a certain period of time. Throughthe annealing treatment, the enhanced reduced Ba-I region 13 a with theR value improved from 0.12 to 0.14 is obtained.

FIG. 7A through FIG. 7E illustrate a semiconductor device fabricationprocess, which device has a thin film capacitor. First, as illustratedin FIG. 7A, MOS transistors 20 are formed in a well region 42 in asemiconductor substrate 40 using a known technique. The well region 42is isolated from the adjacent well regions by isolations (such as STI)41. A cover film (such as SiON film) 21 is formed over the entiresurface to protect the MOS transistors 20. Then, a first interleveldielectric layer 22 is deposited. Contact plugs 30 are formed in thefirst interlevel dielectric layer 22 so as to reach the impuritydiffused regions 20 a of the MOS transistors 20. The contact plug 30 maybe formed by sputtering a TiN/Ti glue layer 30 a in a contact hole (notshown) formed in the interlevel dielectric layer 22, then filling thecontact hole with a tungsten (W) layer 30 b by CVD, and then flatteringthe top surface by CMP.

Then, as illustrated in FIG. 7B, a TiO2 adhesion layer 31 is depositedover the entire surface by a suitable deposition method, such as RFmagnetron sputtering. Then, a Pt film 52 with a thickness of 100 nm anda BST film 53 with a thickness of 100 nm are deposited successively byRF magnetron sputtering. The composition of the BST film 53 is(Ba_(0.7)Sr_(0.3))TiO₃. In the As-Deposition, perovskite-phase Ba-I andnon-perovskite-phase B-II coexist in the surface area of the BST film53. Then, acid cleaning is performed to clean the surface of the BSTfilm 53. With the acid cleaning, Ba-II is removed, while Ba-I stays inthe BST film 53.

Then, as illustrated in FIG. 7C, a 100-nm-thick Pt film 54 is formedover the cleaned surface of the BST film 53 by sputtering orelectron-beam deposition. By controlling the deposition power and/or thepressure, a reduced Ba-I region 53 a, in which concentration ratio ofperovskite-phase Ba-I is less that that of non-perovskite-phase Ba-II,is produced in the surface area of the BST film 53. The relative ratio Rexpressed as (atom % Ba-I)/[(atom % Ba-I)+(atom % Ba-II)] in the reducedBa-I region 53 a is 0.12 (R=0.12) in this example achieved by settingthe power and the pressure to 100 W and 0.1 Pa, respectively, during theformation of the Pt film 54. The deposition conditions for generatingthe reduced Ba-I region 53 a in the BST film 53 may be controlledthroughout or a part of the Pt film deposition process.

Then, as illustrated in FIG. 7D, the Pt film 54, the BST film 53, the Ptfilm 52 and the TiO2 film 31 are patterned by a standardphotolithography process to form a thin film capacitor 10. The thin filmcapacitor 10 comprises a top electrode 14, a bottom electrode 12, and aBST dielectric film 53 held between the top and bottom electrodes. TheBST dielectric film 53 includes the reduced Ba-I region 53 a formed nearthe boundary with the top electrode 54 and a bulk region 53 b ofconstant compositions.

Then, as illustrated in FIG. 7E, an aluminum (Al) protection film 100 isformed over the entire surface, and annealing treatment is performed onthe thin film capacitor 10 at 400° C. in O2 atmosphere for 15 minutes toimprove the R value to 0.14 (R=0.14). As a result, the BST film 63having the enhanced reduced Ba-I region 63 a is obtained.

Although not illustrated in the drawings, another interlevel dielectriclayer is formed over the Al protection film 100. A contact plug (notshown) electrically connected to the lower-level contact plug 30 and acontact plug (not shown) connected to the top electrode 14 of the thinfilm capacitor 10 are formed in the interlevel dielectric layer, andupper-level metal wirings are formed over the flat surface of theinterlevel dielectric layer to complete a semiconductor device 1 withintegrated thin film capacitors 10.

FIG. 8 is a graph of the leakage current density as a function ofapplied voltage, showing superior performance for a structure with Rwithin the specified range. As compared with the original BST film withthe R value of 0.9 (R=0.9), the enhanced reduced Ba-I region with the Rvalue of 1.4 (R=0.14) in which the concentration ratio ofperovskite-phase Ba-I is substantially reduced can reduce leakagecurrent density by two orders of magnitude. Along with the reduction ofthe leakage current density, the service life of the thin film capacitor10 is improved.

Although the present invention has been described using specificexamples, the invention is not limited to these example, and manymodifications and substitutions can be made by those with an ordinaryskill in the art. For example, in the embodiment the deposition processof the top Pt electrode film is controlled to reduce the concentrationratio of the perovskite-phase Ba ions (Ba-I) in the boundary regionbetween the top electrode and the BST dielectric film; however, thereduced Ba-I region may be provided at the boundary between the BSTdielectric film and the bottom electrode.

The semiconductor substrate may be composed of a material selected fromthe group consisting of silicon (Si), Ge, SiGe, GaAs, InAs, InP and allother III/V compounds. The adhesion layer structure may be selected fromthe group Pt, Ir, Zr, Ti, TiOx, IrOx, PtOx, ZrOx, TiN, TiAlN, TaN,TaSiN, etc., consisting of noble metals, alloys of noble metals, alloysof noble and non-noble metals, conductive noble metal oxides, insulatingmetal oxides, insulating metal nitrides, conducting metal nitrides, andcombinations, multilayers or mixtures thereof.

The lower electrode structure may be selected from the group Pt, Pd, Ir,Ru, Rh, Re, Os, Au, Ag, Cu, etc., consisting of transition metals, noblemetals, alloys of noble metals, alloys of noble and non-noble metals, orfrom the group PtOx, IrOx, RuOx consisting of conductive oxides, andcombinations, multilayers, or mixtures thereof.

The upper electrode structure may be selected from the group Pt, Pd, Ir,Ru, Rh, Re, Os, Au, Ag, Cu, etc., consisting of transition metals, noblemetals, alloys of noble metals, alloys of noble and non-noble metals, orfrom the group PtOx, IrOx, RuOx SrRuO3, LaNiO3, etc., consisting ofconductive oxides and combinations, multilayers, or mixtures thereof.

Although in the embodiment the thin film capacitor is applied to asemiconductor memory, such as DRAM, it is also applicable to decouplingcapacitors and tunable filter circuits and other suitable devices.

This patent application is based upon and claims the benefit of theearlier filing date of Japanese Patent Application No. 2006-100595 filedMar. 31, 2006, the entire contents of which are incorporated herein byreference.

1. A method for fabricating a thin film capacitor comprising steps of:forming a dielectric film over a bottom electrode, the dielectric filmbeing composed of at least Ba, Sr, Ti, and O at prescribed compositions;controlling a deposition condition of a top electrode when forming thetop electrode over the dielectric film so as to produce a reduced Ba-Iregion in the dielectric film, in which region an average concentrationof perovskite type Ba cations (Ba-I) is less than an averageconcentration of non-perovskite type Ba cations (Ba-II), at or near aboundary between the top electrode and the dielectric film; andannealing the thin film capacitor in a temperature range of 100° C. to900° C. in an oxygen atmosphere after the top electrode is formed. 2.The method of claim 1, wherein the deposition condition is controlledsuch that a ratio R=(atm % Ba-I)/[(atm % Ba-I)+(atm % Ba-II)] is withina range of 0.1<R<0.2.
 3. The method of claim 1, wherein the reduced Ba-Iregion is produced so as to extend to 5.0 nm, and more preferably, to2.5 nm, from the boundary.
 4. The method of claim 2, further comprisinga step of: annealing the thin film capacitor in a temperature range of100° C. to 900° C. in an oxygen atmosphere after the top electrode isformed.
 5. A method for fabricating a semiconductor device comprisingthe steps of: forming a transistor on a semiconductor substrate; forminga thin film capacitor electrically connected to the transistor, the thinfilm capacitor including a dielectric film held between a top electrodeand a bottom electrode, wherein during the formation of the thin filmcapacitor, a reduced Ba-I region is formed in the dielectric film inwhich an average concentration of perovskite type Ba cations (Ba-I) isless than an average concentration of non-perovskite type Ba cations(Ba-II), at or near a boundary between the top electrode and thedielectric film; and annealing the thin film capacitor in a temperaturerange of 100° C. to 900° C. in an oxygen atmosphere.
 6. The method ofclaim 5, the thin film capacitor forming step including a step of:controlling a deposition condition of the top electrode such that in thereduced Ba-I region a ratio R=(atm % Ba-I)/[(atm % Ba-I)+(atm % Ba-II)]is within a range of 0.1<R<0.2.
 7. The method of claim 5, furthercomprising steps of: forming a contact plug for electrically connectingthe transistor to the thin film capacitor; and forming an adhesion layerto be located between the contact plug and the thin film capacitor.